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- NP1078.RASbnd03z13oZ_IONi2Lg-vGxDp8b-TwTZ6oxNN00Tpz0130_assertion type Assertion NP1078.RASbnd03z13oZ_IONi2Lg-vGxDp8b-TwTZ6oxNN00Tpz0130_head.
- NP1078.RASbnd03z13oZ_IONi2Lg-vGxDp8b-TwTZ6oxNN00Tpz0130_assertion description "[New mutations in MID1 provide support for loss of function as the cause of X-linked Opitz syndrome.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1078.RASbnd03z13oZ_IONi2Lg-vGxDp8b-TwTZ6oxNN00Tpz0130_provenance.
- NP1078.RASbnd03z13oZ_IONi2Lg-vGxDp8b-TwTZ6oxNN00Tpz0130_assertion evidence source_evidence_curated NP1078.RASbnd03z13oZ_IONi2Lg-vGxDp8b-TwTZ6oxNN00Tpz0130_provenance.
- NP1078.RASbnd03z13oZ_IONi2Lg-vGxDp8b-TwTZ6oxNN00Tpz0130_assertion SIO_000772 11030761 NP1078.RASbnd03z13oZ_IONi2Lg-vGxDp8b-TwTZ6oxNN00Tpz0130_provenance.
- NP1078.RASbnd03z13oZ_IONi2Lg-vGxDp8b-TwTZ6oxNN00Tpz0130_assertion wasDerivedFrom uniprot-2016 NP1078.RASbnd03z13oZ_IONi2Lg-vGxDp8b-TwTZ6oxNN00Tpz0130_provenance.
- NP1078.RASbnd03z13oZ_IONi2Lg-vGxDp8b-TwTZ6oxNN00Tpz0130_assertion wasGeneratedBy ECO_0000218 NP1078.RASbnd03z13oZ_IONi2Lg-vGxDp8b-TwTZ6oxNN00Tpz0130_provenance.