Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP764349.RAkXIYxbzIMeGLSMygK_H4Q2vrq1pDK1iEL3arSTJpxMo130_assertion> ?p ?o ?g. }
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- NP764349.RAkXIYxbzIMeGLSMygK_H4Q2vrq1pDK1iEL3arSTJpxMo130_assertion type Assertion NP764349.RAkXIYxbzIMeGLSMygK_H4Q2vrq1pDK1iEL3arSTJpxMo130_head.
- NP764349.RAkXIYxbzIMeGLSMygK_H4Q2vrq1pDK1iEL3arSTJpxMo130_assertion description "[Blood samples were collected from 23 probands and 13 affected family members from 23 genetically unrelated Indian families (22 diagnosed as OCA and 1 diagnosed as OA) and analyzed by bidirectional DNA sequencing of the classic OCA genes--tyrosinase (TYR, or oculocutaneous albinism IA), pink eyed dilution (P; or oculocutaneous albinism II (OCA2]), tyrosinase-related protein 1 (TYRP1), solute carrier family 45, member 2 (SLC45A2; or membrane-associated transporter protein [MATP])--and the OA1 gene, G protein-coupled receptor 143 (GPR143).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP764349.RAkXIYxbzIMeGLSMygK_H4Q2vrq1pDK1iEL3arSTJpxMo130_provenance.
- NP764349.RAkXIYxbzIMeGLSMygK_H4Q2vrq1pDK1iEL3arSTJpxMo130_assertion evidence source_evidence_literature NP764349.RAkXIYxbzIMeGLSMygK_H4Q2vrq1pDK1iEL3arSTJpxMo130_provenance.
- NP764349.RAkXIYxbzIMeGLSMygK_H4Q2vrq1pDK1iEL3arSTJpxMo130_assertion SIO_000772 20806075 NP764349.RAkXIYxbzIMeGLSMygK_H4Q2vrq1pDK1iEL3arSTJpxMo130_provenance.
- NP764349.RAkXIYxbzIMeGLSMygK_H4Q2vrq1pDK1iEL3arSTJpxMo130_assertion wasDerivedFrom befree-20150227 NP764349.RAkXIYxbzIMeGLSMygK_H4Q2vrq1pDK1iEL3arSTJpxMo130_provenance.
- NP764349.RAkXIYxbzIMeGLSMygK_H4Q2vrq1pDK1iEL3arSTJpxMo130_assertion wasGeneratedBy ECO_0000203 NP764349.RAkXIYxbzIMeGLSMygK_H4Q2vrq1pDK1iEL3arSTJpxMo130_provenance.